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The Division of Scholarly Integrity and Research Compliance (SIRC) at Virginia Tech is seeking an Animal Care and Use Program (ACUP) Protocol Coordinator to support ACUP, the Institutional Animal Care and Use Committee (IACUC), and university stakeholders.
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The primary responsibility of the Clinical Research Coordinator B (CRCB) in the Department of Ophthalmology is to implement one or more industry sponsored, NIH or investigator initiated clinical trials assuring each study is conducted per protocol and adheres to ICH/GCP guidelines.
$43,919 - $66,183 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Oversees and ensures compliance with regulations, including organizing electronic files and/or filing regulatory documents appropriately; prepares and submits Institutional Review Board (IRB) documents (i.e., Informed Consent, advertisement, protocol and protocol summary); prepares regulatory documents for sponsor.
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Serve as liaison between participants, physician investigators, sponsors of research, IRBs, CSHRI administration, patient care coordinators and insurance companies to assist in protocol interpretation, clinical and safety questions, and pre-authorization questions.
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Report member complaints to Appeals and Grievance team for investigation and follow-up, per protocol. The Health Care Coordinator (HCC) acts an entry point to CareOregon's Regional Care Teams, as well as provides care coordination.
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Prepares study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports. Acts as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within the protocol.
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As the cornerstone of clinical research, the Clinical Research Coordinator is responsible for facilitating protocol related guidance regarding compliance, personnel and other relevant aspects of trials at multiple research sites, medical institutions, CRO's and Sponsors.
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Assist project director in project planning to ensure that pre-established work scope, study protocol, and program requirements are followed. Research Assistant - Research Coordinator Wayne State University is searching for an experienced Research Assistant - Research Coordinator at its Detroit campus location.
Starting at $39,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Model and co-facilitate restorative practices in classrooms and in staff meetings, with an objective of building staff capacity to facilitate, including a restorative discipline protocol to communicate school-wide expectations for restorative justice practices Provide individual and team coaching for administrators and staff to develop restorative justice skills; observe the facilitation of restorative practices and provide constructive feedback.
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The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
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Clinical Research Coordinator - Shafi / Buss Facility: Beth Israel Deaconess Medical Center, 03 / 22
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Identifies any problems with protocol compliance and notifies principal investigator and/or research nurse. Extracts data on protocol subjects from hospital records, outpatient charts and private physician office records in order to complete case report forms required by specific protocols.
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Clinical Research Coordinators at the Depression and Anxiety Center for Discovery and Treatment (DAC) are responsible for administrative, academic and clinical tasks related to conducting a given study, including: running experimental procedures, entering and analyzing data, blood draws, saliva and urine collection, collecting and processing biological specimens, protocol development, as well as preparing presentations, publications or grant applications.
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The CSC will interact telephonically with members as per established protocol or direction to ensure that members are effectively and efficiently managed through the medical/disease management process as needs require and in helping the RN care manager or social worker in arranging appropriate medical equipment (DME), home health, follow-up appointments, and other services related to care coordination.
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Reporting to the Breast CRG Clinical Research Manger, the Clinical Research Coordinator Associate - Breast Oncology will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to ensure protocol requirements are carried out and data quality is maintained.
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Works on sensitive issues, priorities, protocol, et cetera. Program Coordinator (4722C) - 66806. This position is governed by the terms and conditions in the agreement for the Clerical & Allied Services Unit (CX) between the University of California and Teamsters Local 2010.
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protocol job Title: coordinator
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